Keith T. Sillar

3.9k total citations
91 papers, 2.9k citations indexed

About

Keith T. Sillar is a scholar working on Cell Biology, Cellular and Molecular Neuroscience and Ecology. According to data from OpenAlex, Keith T. Sillar has authored 91 papers receiving a total of 2.9k indexed citations (citations by other indexed papers that have themselves been cited), including 59 papers in Cell Biology, 58 papers in Cellular and Molecular Neuroscience and 25 papers in Ecology. Recurrent topics in Keith T. Sillar's work include Zebrafish Biomedical Research Applications (59 papers), Neuroscience and Neuropharmacology Research (33 papers) and Neurobiology and Insect Physiology Research (32 papers). Keith T. Sillar is often cited by papers focused on Zebrafish Biomedical Research Applications (59 papers), Neuroscience and Neuropharmacology Research (33 papers) and Neurobiology and Insect Physiology Research (32 papers). Keith T. Sillar collaborates with scholars based in United Kingdom, United States and France. Keith T. Sillar's co-authors include David L. McLean, Alan Roberts, A. John Simmers, Peter Skorupski, J. Wedderburn, Gareth B. Miles, Laurence D. Picton, Jonathan R. McDearmid, W. J. Heitler and Denis Combes and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Journal of Neuroscience.

In The Last Decade

Keith T. Sillar

91 papers receiving 2.9k citations

Peers

Keith T. Sillar

CMN

ECOLO

Hans J. ten Donkelaar Netherlands

Carl M. Rovainen United States

S. Grillner Sweden

James T. Buchanan United States

David L. McLean United States

Alan Roberts United Kingdom

Pierre Meyrand France

Donald S. Faber United States

Joseph R. Fetcho United States

Claire Wyart France

Hans J. ten Donkelaar Netherlands

Keith T. Sillar

1.4k ×0.8

CMN

893 ×0.7

582 ×0.8

966 ×1.6

411 ×0.8

ECOLO

Citations per year, relative to Keith T. Sillar Keith T. Sillar (= 1×) peers Hans J. ten Donkelaar

Countries citing papers authored by Keith T. Sillar

Since Specialization

Citations

This map shows the geographic impact of Keith T. Sillar's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Keith T. Sillar with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Keith T. Sillar more than expected).

Fields of papers citing papers by Keith T. Sillar

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Keith T. Sillar. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Keith T. Sillar. The network helps show where Keith T. Sillar may publish in the future.

Co-authorship network of co-authors of Keith T. Sillar

This figure shows the co-authorship network connecting the top 25 collaborators of Keith T. Sillar. A scholar is included among the top collaborators of Keith T. Sillar based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Keith T. Sillar. Keith T. Sillar is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Picton, Laurence D., et al.. (2022). Bimodal modulation of short-term motor memory via dynamic sodium pumps in a vertebrate spinal cord. Current Biology. 32(5). 1038–1048.e2. 8 indexed citations

Picton, Laurence D., Keith T. Sillar, & Hongyan Zhang. (2018). Control of Xenopus Tadpole Locomotion via Selective Expression of Ih in Excitatory Interneurons. Current Biology. 28(24). 3911–3923.e2. 19 indexed citations

Zhang, Hongyan, Laurence D. Picton, Wenchang Li, & Keith T. Sillar. (2015). Mechanisms underlying the activity-dependent regulation of locomotor network performance by the Na+ pump. Scientific Reports. 5(1). 16188–16188. 28 indexed citations

Zhang, Hongyan & Keith T. Sillar. (2012). Short-Term Memory of Motor Network Performance via Activity-Dependent Potentiation of Na+/K+ Pump Function. Current Biology. 22(6). 526–531. 48 indexed citations

Sillar, Keith T. & R. Meldrum Robertson. (2009). Thermal activation of escape swimming in post-hatching Xenopus laevis frog larvae. Journal of Experimental Biology. 212(15). 2356–2364. 27 indexed citations

Sillar, Keith T.. (2009). Escape Behaviour: Reciprocal Inhibition Ensures Effective Escape Trajectory. Current Biology. 19(16). R697–R699. 5 indexed citations

Sillar, Keith T.. (2009). Mauthner cells. Current Biology. 19(9). R353–R355. 36 indexed citations

Kyriakatos, Alexandros, Marco Molinari, Riyadh Mahmood, et al.. (2009). Nitric Oxide Potentiation of Locomotor Activity in the Spinal Cord of the Lamprey. Journal of Neuroscience. 29(42). 13283–13291. 35 indexed citations

Ramanathan, Sankari, et al.. (2006). Developmental and regional expression of NADPH‐diaphorase/nitric oxide synthase in spinal cord neurons correlates with the emergence of limb motor networks in metamorphosing Xenopus laevis. European Journal of Neuroscience. 24(7). 1907–1922. 19 indexed citations

10.

McLean, David L. & Keith T. Sillar. (2004). Metamodulation of a Spinal Locomotor Network by Nitric Oxide. Journal of Neuroscience. 24(43). 9561–9571. 57 indexed citations

11.

McLean, David L. & Keith T. Sillar. (2004). Divergent actions of serotonin receptor activation during fictive swimming in frog embryos. Journal of Comparative Physiology A. 190(5). 391–402. 17 indexed citations

12.

McDearmid, Jonathan R., et al.. (2003). Mechanisms underlying the noradrenergic modulation of longitudinal coordination during swimming in Xenopus laevis tadpoles. European Journal of Neuroscience. 17(5). 1013–1022. 8 indexed citations

13.

Fischer, Hanno, et al.. (2001). Adrenoreceptor‐mediated modulation of the spinal locomotor pattern during swimming in Xenopus laevis tadpoles. European Journal of Neuroscience. 13(5). 977–986. 11 indexed citations

14.

McDearmid, Jonathan R., et al.. (1997). Aminergic Modulation of Glycine Release in a Spinal Network Controlling Swimming in Xenopus Laevis. The Journal of Physiology. 503(1). 111–117. 66 indexed citations

15.

Sillar, Keith T., et al.. (1995). Involvement of brainstem serotonergic interneurons in the development of a vertebrate spinal locomotor circuit. Proceedings of the Royal Society B Biological Sciences. 259(1354). 65–70. 47 indexed citations

16.

Wedderburn, J. & Keith T. Sillar. (1994). Modulation of rhythmic swimming activity in post-embryonic Xenopus laevis tadpoles by 5-hydroxytryptamine acting at 5HT _1a receptors. Proceedings of the Royal Society B Biological Sciences. 257(1348). 59–66. 19 indexed citations

17.

Wedderburn, J., et al.. (1994). Descending serotonergic spinal projections and modulation of locomotor rhythmicity in Rana temporaria embryos. Proceedings of the Royal Society B Biological Sciences. 255(1342). 73–79. 36 indexed citations

18.

Sillar, Keith T., et al.. (1991). Segregation of NMDA and non-NMDA receptors at separate synaptic contacts: evidence from spontaneous EPSPs inXenopus embryo spinal neurons. Brain Research. 545(1-2). 24–32. 17 indexed citations

19.

Sillar, Keith T., J. Wedderburn, & A. John Simmers. (1991). The development of swimming rhythmicity in post-embryonic Xenopus laevis. Proceedings of the Royal Society B Biological Sciences. 246(1316). 147–153. 69 indexed citations

20.

Roberts, Alan & Keith T. Sillar. (1990). Characterization and Function of Spinal Excitatory Interneurons with Commissural Projections in Xenopus laevis embryos. European Journal of Neuroscience. 2(12). 1051–1062. 53 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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